A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441711



Internal ID22499581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24757169..24757581hg38UCSC Ensembl
chr7:24796788..24797200hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914865
Supporting Variants
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441711
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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